ibuprofen
- Product NDC
- 68788-8182
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ibuprofen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA202413
- Marketing category
- ANDA
- Substance
- IBUPROFEN
- Current FDA listing
- Historical FDA.report record
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68788-8182-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8182-1) | 2022-04-28 | 0000-00-00 | No | Current |
| 68788-8182-2 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-8182-2) | 2022-04-28 | 0000-00-00 | No | Current |
| 68788-8182-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8182-3) | 2022-04-28 | 0000-00-00 | No | Current |
| 68788-8182-4 | 14 TABLET, FILM COATED in 1 BOTTLE (68788-8182-4) | 2022-04-28 | 0000-00-00 | No | Current |
| 68788-8182-5 | 50 TABLET, FILM COATED in 1 BOTTLE (68788-8182-5) | 2022-04-28 | 0000-00-00 | No | Current |
| 68788-8182-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8182-6) | 2022-04-28 | 0000-00-00 | No | Current |
| 68788-8182-7 | 21 TABLET, FILM COATED in 1 BOTTLE (68788-8182-7) | 2022-04-28 | 0000-00-00 | No | Current |
| 68788-8182-8 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-8182-8) | 2022-04-28 | 0000-00-00 | No | Current |
| 68788-8182-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8182-9) | 2022-04-28 | 0000-00-00 | No | Current |